Variant #0001027336 (NC_000020.10:g.61450663_61450665dup, NC_000020.10(NM_001853.3):c.255+18_255+20dup (COL9A3))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61450663_61450665dup
DNA change (hg38) -
Published as COL9A3(NM_001853.4):c.255+16_255+18dupCCT
ISCN -
DB-ID COL9A3_000136
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
COL9A3 NM_001853.3 -/. - c.255+18_255+20dup r.(=) p.(=)
TCFL5 NM_006602.2 -/. - c.*22664_*22666dup r.(=) p.(=)


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